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Job Details

Clinical Trial Manager

Company: CROMSOURCE
Location: East Coast, United States
Reference: HQ00001653
Closing Date: 22 Feb 19
Type: Permanent
Salary (£): On Application
Benefits: Excellent and Comprehensive Benefits – see below

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Job Summary:

:  Clinical Trial Manager       :  Remote/East Coast-United States; Boston, Massachussetts preferred   Schedule:  Full Time, 40 hours/week         CROMSOURCE is looking for a Clinical Trial Manager to join one of our partner Pharmaceutical companies, who specialize in Genetic and Rare Diseases, along the East Coast of the US preferably in the Boston area.

Requirements:

Job Title: Clinical Trial Manager

Location: Remote/East Coast-United States; Boston, Massachussetts preferred

Schedule: Full Time, 40 hours/week

CROMSOURCE is looking for a Clinical Trial Manager to join one of our partner Pharmaceutical companies, who specialize in Genetic and Rare Diseases, along the East Coast of the US preferably in the Boston area.

This will be a full time, permanent opportunity and the successful candidate will be working on studies dedicated to one client.

For our client-facing positions, you must be confident and be able to drive the role and yourself and to work autonomously. You will have a close relationship with our Line Managers, who will provide you with mentoring and guidance. Most of our roles are permanent positions with CROMSOURCE and you will be working on studies for just one client. We are open, friendly and approachable and aim to support you through the recruitment process every step of the way.

Must have experience with study-start up activities and experience with CRO oversight.

Key accountabilities: 

  • Maintains budget, addressing issues as appropriate.
  • Ensures appropriate clinical trial supply strategy and recruitment plan is implemented, manages risk, monitors progress.
  • Ensures adherence to Good Clinical Practice and all applicable local and international regulations.
  • Ensures delivery of high quality study documents in order to meet study timelines.
  • Manages clinical vendor and contractual agreements.
  • Drives assessment, selection, engagement, training and management of appropriate vendors for outsourced clinical activities/services, ensuring compliance with standards.
  • Accountable for site and monitor training in operational aspects of the study.
  • Ensures monitoring and site personnel are familiar with all study-specific processes, procedures and systems and that training is adequately documented.
  • Accountable for study related communications and for resolution or escalation of operational issues.
  • Ensures accurate maintenance and archiving of study records.

Skills

  • Excellent interpersonal, verbal and written communication skills.
  • Client focused approach to work.
  • A flexible attitude with respect to work assignments and new learning.
  • Ability to effectively and proactively manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail.
  • Willingness to work in a matrix environment and to value the importance of teamwork
  • Possess strong negotiation, diplomacy, team leadership skills and excellent organizational ability.
  • Excellent problem solving capability through early identification.
  • Demonstrate, appreciation and understanding of finance and budgeting issues.

If you have the experience needed for this position, please apply directly to https://www.talentsourcelifesciences.com/job-information/?job-id=Hq00001653. If you would like to discuss the role before applying through the website, please contact Laura.Guascone@cromsource.com for more information.

The Benefits of Working for TalentSource in the US

  • Full health insurance benefits that include health, dental and vision
  • 401K Plan with 5% company match after satisfying 90 days of employment
  • Short term and long term disability insurance
  • Life insurance
  • Paid vacation, sick leave and holidays
  • Dedicated Line Manager
  • Monthly meetings with line manager
  • Full performance and development process with
  • Team events and end of year party
  • Career opportunities within both our CRO departments and our TalentSource Life Sciences Unit, locally and internationally
  • Employee satisfaction survey - your feedback is important for continuous improvement

Why choose TalentSource Life Sciences/CROMSOURCE?

TalentSource Life Sciences is a fully dedicated flexible resourcing department at CROMSOURCE, a family owned international, full-service Contract Research Organization. CROMSOURCE comes from the merger of MSOURCE and CROM and we have been supporting clients with outstanding clinical research and resourcing services since 1994. Successful growth has been achieved by putting high quality and client focus at the heart of everything we do and we are proud to partner with industry leading Pharmaceutical, Biotechnology, Medical Device and Marketing Communications worldwide.

Our employees are the most valuable company asset and because we want to retain our staff, we ensure they work in a friendly, family environment and develop their skills and talents. Human Resources is the fulcrum around which all activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertize and gives to all personnel clear tools to manage both internal and client processes with the same methodology. The success of these core values are evidenced by our current below industry average turnover rates.

Our approach is to equally value our clients and our own people. We know that we are not simply providing 'staff' or 'resources'. We are experts providing experts - highly talented, well trained, motivated people who make a positive difference to the work of our clients every day. Together we help our clients succeed in their work developing medicines and medical devices for patients around the world.

Key skills: Clinical Trial Manager, CTM, Junior Project Manager, Junior CTM, Project Manager, Study Manager, Clinical Study Manager, Clinical Project Manager, CPM, CSM, PM, SM, Lead CRA, LCRA, Lead Clinical Research Associate, Permanent, Contract Research Organization, CRO, Outsourced, Pharma, Pharmaceutical

Clinical Project Manager, Clinical Study Manager, Clinical Trial Manager, Lead Clinical Research Associate

Apply for this job: Clinical Trial Manager

Contact Information:

Address:  UK Office
CROMSOURCE Suite 3 Lomond Court Castle Business Park Stirling United Kingdom
FK9 4TU
Scotland
Tel:  +44 (0) 1786 468990
Website:  Visit Our Web Site

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